methylphenidate hydrochloride
- Product NDC
- 0591-2718
- 11-digit product format
- 005912718
- Labeler code
- 0591
- Product ID
- 0591-2718_6b2dcacd-6280-421e-8ac2-ac00db79a5d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA021121
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-04-01
- Marketing end
- 2021-09-30
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 54 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-2718-01 | 00591271801 | 100 TABLET in 1 BOTTLE (0591-2718-01) | 100 tablet | 2011-04-01 | 2021-09-30 | No | No | Current |